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Spatial Functional Characteristics of East Asian Patients With Occult Macular Dystrophy (Miyake Disease); EAOMD Report No. 2.
- Source :
-
American journal of ophthalmology [Am J Ophthalmol] 2021 Jan; Vol. 221, pp. 169-180. Date of Electronic Publication: 2020 Jul 21. - Publication Year :
- 2021
-
Abstract
- Purpose: To describe the functional phenotypic features of East Asian patients with RP1L1-associated occult macular dystrophy (ie, Miyake disease).<br />Design: An international multicenter retrospective cohort study.<br />Methods: Twenty-eight participants (53 eyes) with Miyake disease were enrolled at 3 centers (in Japan, China, and South Korea). Ophthalmologic examinations including spectral-domain optical coherence tomography (SDOCT) and multifocal electroretinogram (mfERG) were performed. Patients were classified into 3 functional groups based on mfERG: Group 1, paracentral dysfunction with relatively preserved central/peripheral function; Group 2, homogeneous central dysfunction with preserved peripheral function; and Group 3, widespread dysfunction over the recorded area. Three functional phenotypes were compared in clinical parameters and SDOCT morphologic classification (severe phenotype, blurred/flat ellipsoid zone and absence of the interdigitation zone; mild phenotype, preserved ellipsoid zone).<br />Results: There were 8 eyes in Group 1, 40 eyes in Group 2, and 5 eyes in Group 3. The patients in Group 1 showed significantly later onset (P = .005) and shorter disease duration (P = .002), compared with those in Group 2. All 8 eyes in Group 1 showed the mild morphologic phenotype, while 43 of 45 eyes in Groups 2 and 3 presented the severe phenotype, which identified a significant association between the functional grouping and the morphologic classification (P < .001).<br />Conclusions: A spectrum of functional phenotypes of Miyake disease was first documented with identification of 3 functional subtypes. Patients with paracentral dysfunction had the mildest phenotype, and those with homogeneous central or widespread dysfunction showed overlapping clinical findings with severe photoreceptor changes, suggesting various extents of visual impairment.<br /> (Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Adolescent
Adult
Aged
Aged, 80 and over
Asian People genetics
Child
Electroretinography
Eye Proteins genetics
Female
Fluorescein Angiography
Humans
Macular Degeneration genetics
Male
Middle Aged
Phenotype
Retrospective Studies
Spatial Navigation physiology
Tomography, Optical Coherence
Visual Acuity physiology
Exome Sequencing
Young Adult
Macular Degeneration physiopathology
Retina physiopathology
Subjects
Details
- Language :
- English
- ISSN :
- 1879-1891
- Volume :
- 221
- Database :
- MEDLINE
- Journal :
- American journal of ophthalmology
- Publication Type :
- Academic Journal
- Accession number :
- 32707201
- Full Text :
- https://doi.org/10.1016/j.ajo.2020.07.025